TRACE: Thymosin Alpha 1 in the Prevention of Pancreatic Infection Following Acute Necrotizing Pancreatitis

Sponsor
Weiqin Li (Other)
Overall Status
Completed
CT.gov ID
NCT02473406
Collaborator
The First Affiliated Hospital of Nanchang University (Other), The Affiliated Hospital of Qingdao University (Other), Zunyi Medical College (Other), the Affiliated Nanhua Hospital, University of South China (Other), Second Affiliated Hospital of Nantong University (Other), Yijishan Hospital of Wannan Medical College (Other), the 908th Hospital of Chinese People's Liberation Army Joint Logistic Support Force (Other), Jiangsu Province Hospital of Traditional Chinese Medicine (Other), Zhejiang Provincial People's Hospital (Other), Luoyang Central Hospital (Other), The Affiliated Hospital of Henan University of Science and Technology (Other), Clinical Medical College of Yangzhou University (Other), The First People's Hospital of Shangqiu (Other), Qilu Hospital of Shandong University (Other), The First Affiliated Hospital of Anhui Medical University (Other)
508
2
2
35.9
254
7.1

Study Details

Study Description

Brief Summary

Infected pancreatic necrosis and its related septic complications are the major cause of death in patients with acute pancreatitis, therefore prevention of pancreatic infection is of great clinical value in the treatment of AP.

Immunosuppression and disorders characterized by decreased HLA-DR expression and unbalanced CD3/CD4+/CD8+ T cells of PBMC are thought to be associated with the development of pancreatic infection. Thymosin alpha 1 has been shown to have immunomodulatory properties and its effects in preventing pancreatic infection was not well studied. To evaluate the effects of TA1 use in the early phase on preventing pancreatic infection, immunomodulation and clinical outcomes in patients with AP,we aimed to design this study.

Condition or Disease Intervention/Treatment Phase
  • Drug: Thymosin Alpha 1
  • Drug: normal saline
Phase 4

Detailed Description

Study Background & Rationale:

Infected pancreatic necrosis and its related septic complications are the major cause of death in patients with acute pancreatitis1, therefore prevention of pancreatic infection is of great clinical value in the treatment of AP.

Immunosuppression and disorders characterized by decreased HLA-DR expression and unbalanced CD3/CD4+/CD8+ T cells of PBMC are thought to be associated with the development of pancreatic infection2, 3. Thymosin alpha 1 has been shown to have immunomodulatory properties and its effects in preventing pancreatic infection was not well studied4.

Aim of This Study:

To evaluate the effects of TA1 use in the early phase on preventing pancreatic infection, immunomodulation and clinical outcomes in patients with AP.

Sample Size Estimation:

The prevalence of pancreatic infection was reported to be around 25% in AP episodes. To demonstrate a 40% reduction in the prevalence of pancreatic infection with 80% power at a two-sided alpha level of .05, we projected an estimated sample size of 500 participants. Considering possible 2% withdraw, we plan to randomize 510 patients in total.

Study Design

Study Type:
Interventional
Actual Enrollment :
508 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
Primary Purpose:
Prevention
Official Title:
Thymosin Alpha 1 in the Prevention of Pancreatic Infection Following Acute Necrotizing Pancreatitis
Actual Study Start Date :
Mar 27, 2018
Actual Primary Completion Date :
Dec 24, 2020
Actual Study Completion Date :
Mar 24, 2021

Arms and Interventions

Arm Intervention/Treatment
Experimental: Thymosin

Thymosin alpha 1 has been shown to have immunomodulatory properties

Drug: Thymosin Alpha 1
In addition to the standard treatment, thymosin therapy will be started after admission: 1.6mg I.H q12h for the first 7 days and 1.6mg I.H, qd for the following 7 days or until discharge.
Other Names:
  • Thymosin Group
  • Placebo Comparator: Placebo

    normal saline;

    Drug: normal saline
    Placebo inject will be given at the same dose as Thymosin in addition to the standard treatment.
    Other Names:
  • Placebo Group
  • Outcome Measures

    Primary Outcome Measures

    1. Occurrence of pancreatic infection: [during the index admission]

    Secondary Outcome Measures

    1. The occurrence of new-onset organ failure and new-onset persistent organ failure [during the index admission]

      (SOFA score for respiration, cardiovascular, or renal system ≥2 ). New-onset is defined as events that occur after randomization and not present 24 hours before randomization

    2. In-hospital mortality [during the index admission]

    3. Bleeding requiring intervention [during the index admission]

    4. Gastrointestinal perforation or fistula requiring intervention [during the index admission]

    5. Incidence of pancreatic fistula [during the index admission]

    6. New receipt of mechanical ventilation/renal replacement therapy /New receipt of vasoactive agents [during the index admission]

      not applied 24 hours before randomization

    7. The requirement for catheter drainage/Number of drainage procedures required [during the index admission]

    8. The requirement for minimally-invasive debridement/Number of minimally invasive necrosectomy required [during the index admission]

    9. The requirement for open surgery/Number of open surgery required [during the index admission]

    10. Length of intensive care unit(ICU) stay/Length of hospital stay [during the index admission]

    11. SOFA score/ CRP level/ HLA-DR level/ Lymphocyte count [on day0, day7, and day14]

    12. In-hospital cost. [during the index admission]

    13. Incidence of infection within 90 days after enrollment [90 days after enrollment]

    14. Mortality within 90 days after enrollment [90 days after enrollment]

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 70 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No

    Inclusion criteria

    1. Symptoms and signs of acute pancreatitis based on abdominal pain suggestive of AP, serum amylase at least three times the upper limit of normal, and/or characteristic findings of AP on computed tomography or less commonly magnetic resonance imaging (MRI) or transabdominal ultrasonography according to the Revised Atlanta Criteria[15];

    2. Less than one week from the onset of abdominal pain;

    3. Age between 18 to 70 years old;

    4. Acute Physiology and Chronic Health Evaluation(APACHE II) score ≥8 during the last 24 hours before enrollment

    5. Balthazar CT score ≥5 (presence of pancreatic necrosis)[16].

    6. Written informed consent obtained

    Exclusion criteria

    1. Pregnant pancreatitis;

    2. History of chronic pancreatitis;

    3. Malignancy related acute pancreatitis

    4. Receiving early intervention or surgery due to abdominal compartment syndrome or other reasons before admission;

    5. Patients with a known history of severe cardiovascular, respiratory, renal or hepatic diseases defined as (1) greater than New York Heart Association Class II heart failure(Class II not included), (2) active myocardial ischemia or (3) cardiovascular intervention within previous 60 days, (4) history of cirrhosis or (5) chronic kidney disease with creatinine clearance< 40 mL/min, or (6) chronic obstructive pulmonary disease with requirement for home oxygen;

    6. Patients with preexisting immune disorders such as AIDS.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Department of SICU, Research Institute of General Surgery Jinling Hospital, Nanjing, Jiangsu, China Nanjing Jiangsu China 210002
    2 Jinling Hospital Nanjing Jiangsu China 210010

    Sponsors and Collaborators

    • Weiqin Li
    • The First Affiliated Hospital of Nanchang University
    • The Affiliated Hospital of Qingdao University
    • Zunyi Medical College
    • the Affiliated Nanhua Hospital, University of South China
    • Second Affiliated Hospital of Nantong University
    • Yijishan Hospital of Wannan Medical College
    • the 908th Hospital of Chinese People's Liberation Army Joint Logistic Support Force
    • Jiangsu Province Hospital of Traditional Chinese Medicine
    • Zhejiang Provincial People's Hospital
    • Luoyang Central Hospital
    • The Affiliated Hospital of Henan University of Science and Technology
    • Clinical Medical College of Yangzhou University
    • The First People's Hospital of Shangqiu
    • Qilu Hospital of Shandong University
    • The First Affiliated Hospital of Anhui Medical University

    Investigators

    • Study Chair: Li Weiqin, M.D., Department of SICU, Research Institute of General Surgery Jinling Hospital, Nanjing, Jiangsu, Chin
    • Study Director: Ke Lu, M.D., Department of SICU, Research Institute of General Surgery Jinling Hospital, Nanjing, Jiangsu, Chin
    • Principal Investigator: Zhou Jing, M.D., Department of SICU, Research Institute of General Surgery Jinling Hospital, Nanjing, Jiangsu, Chin

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Weiqin Li, Professor, Nanjing University School of Medicine
    ClinicalTrials.gov Identifier:
    NCT02473406
    Other Study ID Numbers:
    • TRACE trial
    First Posted:
    Jun 16, 2015
    Last Update Posted:
    Apr 5, 2021
    Last Verified:
    Apr 1, 2021
    Individual Participant Data (IPD) Sharing Statement:
    Undecided
    Plan to Share IPD:
    Undecided
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Weiqin Li, Professor, Nanjing University School of Medicine
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Apr 5, 2021